NZ542396A - Novel method for the synthesis of S-indoline-2-carboxylic acid and application thereof in the synthesis of perindopril - Google Patents
Novel method for the synthesis of S-indoline-2-carboxylic acid and application thereof in the synthesis of perindoprilInfo
- Publication number
- NZ542396A NZ542396A NZ542396A NZ54239604A NZ542396A NZ 542396 A NZ542396 A NZ 542396A NZ 542396 A NZ542396 A NZ 542396A NZ 54239604 A NZ54239604 A NZ 54239604A NZ 542396 A NZ542396 A NZ 542396A
- Authority
- NZ
- New Zealand
- Prior art keywords
- formula
- indoline
- carboxylic acid
- yield
- isomer
- Prior art date
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D209/00—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
- C07D209/02—Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
- C07D209/04—Indoles; Hydrogenated indoles
- C07D209/30—Indoles; Hydrogenated indoles with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, directly attached to carbon atoms of the hetero ring
- C07D209/42—Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61K—PREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
- A61K31/00—Medicinal preparations containing organic active ingredients
- A61K31/33—Heterocyclic compounds
- A61K31/395—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
- A61K31/40—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
- A61K31/403—Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
- A61K31/404—Indoles, e.g. pindolol
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B55/00—Racemisation; Complete or partial inversion
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
- C07B2200/07—Optical isomers
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Life Sciences & Earth Sciences (AREA)
- Pharmacology & Pharmacy (AREA)
- Epidemiology (AREA)
- Medicinal Chemistry (AREA)
- Animal Behavior & Ethology (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Indole Compounds (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
- Peptides Or Proteins (AREA)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
EP03290879A EP1348684B1 (fr) | 2003-04-09 | 2003-04-09 | Nouveau procédé de synthèse de l'acide (2S)-indoline-2-carboxilique, et application à la synthèse du perindopril |
PCT/FR2004/000857 WO2004092095A1 (fr) | 2003-04-09 | 2004-04-07 | Nouveau procede de synthese de l'acide (2s)-indoline-2- carboxylique, et application a la synthese du perindopril |
Publications (1)
Publication Number | Publication Date |
---|---|
NZ542396A true NZ542396A (en) | 2010-03-26 |
Family
ID=27798985
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
NZ542396A NZ542396A (en) | 2003-04-09 | 2004-04-07 | Novel method for the synthesis of S-indoline-2-carboxylic acid and application thereof in the synthesis of perindopril |
Country Status (28)
Country | Link |
---|---|
US (2) | US7196204B2 (da) |
EP (1) | EP1348684B1 (da) |
JP (1) | JP5111849B2 (da) |
KR (1) | KR100722079B1 (da) |
CN (1) | CN100337996C (da) |
AR (1) | AR043993A1 (da) |
AT (1) | ATE319668T1 (da) |
AU (1) | AU2004230294B2 (da) |
BR (1) | BRPI0409095B1 (da) |
CA (1) | CA2521877C (da) |
DE (1) | DE60303904T2 (da) |
DK (1) | DK1348684T3 (da) |
EA (1) | EA008929B1 (da) |
EG (1) | EG24152A (da) |
ES (1) | ES2260585T3 (da) |
GE (1) | GEP20074257B (da) |
HK (1) | HK1086816A1 (da) |
MA (1) | MA27633A1 (da) |
MX (1) | MXPA05010398A (da) |
MY (1) | MY138698A (da) |
NO (1) | NO334199B1 (da) |
NZ (1) | NZ542396A (da) |
PL (1) | PL212544B1 (da) |
PT (1) | PT1348684E (da) |
SI (1) | SI1348684T1 (da) |
UA (1) | UA80040C2 (da) |
WO (1) | WO2004092095A1 (da) |
ZA (1) | ZA200507567B (da) |
Families Citing this family (10)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
SI1348684T1 (sl) * | 2003-04-09 | 2006-06-30 | Servier Lab | Nov postopek sinteze (2s)-indolin-2-karboksilne kisline in uporaba pri sintezi perindoprila |
CA2488324A1 (en) * | 2004-11-22 | 2006-05-22 | Apotex Pharmachem Inc. | Optical resolution of n-acetyl-indoline-2-carboxylic acid with phenylglycinol |
CN100391945C (zh) * | 2005-05-31 | 2008-06-04 | 浙江大学 | 一种s-(-)-吲哚啉-2-羧酸的合成方法 |
EP1792896A1 (en) | 2005-12-01 | 2007-06-06 | KRKA, tovarna zdravil, d.d., Novo mesto | Process for the preparation of perindopril and salts thereof |
JP5176452B2 (ja) * | 2007-09-27 | 2013-04-03 | 住友化学株式会社 | 光学活性なテトラヒドロピラニルグリシン化合物の製造方法 |
CN101774960B (zh) * | 2009-12-31 | 2011-08-03 | 安徽美诺华药物化学有限公司 | 一种(2s)-二氢吲哚-2-甲酸的制备方法 |
CN101823993A (zh) * | 2010-03-31 | 2010-09-08 | 安徽世华化工有限公司 | L-八氢吲哚啉-2-甲酸的制备方法 |
CN104672124B (zh) * | 2014-12-31 | 2017-08-22 | 浙江昌明药业有限公司 | 对映体富集的二氢吲哚‑2‑甲酸的合成方法 |
CN112321538A (zh) * | 2020-10-28 | 2021-02-05 | 都创(上海)医药开发有限公司 | 一种合成单胺保护的哌嗪-(r/s)2-甲酸酯的方法 |
CN112375028A (zh) * | 2020-12-14 | 2021-02-19 | 安徽美诺华药物化学有限公司 | 合成(2s)-二氢吲哚-甲酸的方法 |
Family Cites Families (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS535134A (en) * | 1976-06-30 | 1978-01-18 | Sumitomo Chem Co Ltd | Racemization of optical active 2-(4)chlorophenyl)-3-methylbutylic acid |
JPS58216147A (ja) * | 1982-06-11 | 1983-12-15 | Banyu Pharmaceut Co Ltd | 光学活性なn−アセチル−3−ヒドロキシ−4−(ヒドロキシメチル)フエニルグリシンのラセミ化方法 |
DE3571969D1 (en) * | 1984-05-30 | 1989-09-07 | Du Pont | Preparation of optically-active alpha-substituted phenylacetic acids |
DE3727411A1 (de) * | 1986-08-19 | 1988-03-24 | Ciba Geigy Ag | Verfahren zur herstellung von 2-indolincarbonsaeure |
JPH0780823B2 (ja) * | 1986-08-26 | 1995-08-30 | 東ソー株式会社 | 光学活性フェニルアラニンのラセミ化方法 |
FR2620709B1 (fr) * | 1987-09-17 | 1990-09-07 | Adir | Procede de synthese industrielle du perindopril et de ses principaux intermediaires de synthese |
JP2513001B2 (ja) * | 1988-11-01 | 1996-07-03 | 山川薬品工業株式会社 | 光学活性テトラヒドロフラン−2−カルボン酸のラセミ化方法 |
JP3010694B2 (ja) * | 1990-07-09 | 2000-02-21 | 日産化学工業株式会社 | 2―(3―ベンゾイル)フェニルプロピオン酸のラセミ化法 |
NL9001703A (nl) * | 1990-07-27 | 1992-02-17 | Westspur Investment Ltd | Werkwijze voor de bereiding van s(+)-6-methoxy-alfa-methyl-2-naftaleen-azijnzuur. |
US5220053A (en) * | 1992-01-24 | 1993-06-15 | Ethyl Corporation | Preparation of optically active aliphatic carboxylic acids |
ES2061403B1 (es) * | 1993-04-16 | 1995-06-16 | Medichem Sa | Procedimiento de obtencion del acido d-(-) -3 acetiltio-2- metilpropionico. |
JPH08151344A (ja) * | 1994-09-26 | 1996-06-11 | Nagase & Co Ltd | 2−(3−ベンゾイルフェニル)プロピオン酸の光学分割方法 |
US5677469A (en) * | 1995-05-18 | 1997-10-14 | Sepracor, Inc. | Process for resolving chiral acids with 1-aminoindan-2-ols |
SI1348684T1 (sl) * | 2003-04-09 | 2006-06-30 | Servier Lab | Nov postopek sinteze (2s)-indolin-2-karboksilne kisline in uporaba pri sintezi perindoprila |
-
2003
- 2003-04-09 SI SI200330204T patent/SI1348684T1/sl unknown
- 2003-04-09 ES ES03290879T patent/ES2260585T3/es not_active Expired - Lifetime
- 2003-04-09 DE DE60303904T patent/DE60303904T2/de not_active Expired - Lifetime
- 2003-04-09 AT AT03290879T patent/ATE319668T1/de active
- 2003-04-09 PT PT03290879T patent/PT1348684E/pt unknown
- 2003-04-09 DK DK03290879T patent/DK1348684T3/da active
- 2003-04-09 EP EP03290879A patent/EP1348684B1/fr not_active Expired - Lifetime
-
2004
- 2004-04-07 US US10/552,676 patent/US7196204B2/en not_active Expired - Fee Related
- 2004-04-07 NZ NZ542396A patent/NZ542396A/en not_active IP Right Cessation
- 2004-04-07 ZA ZA200507567A patent/ZA200507567B/xx unknown
- 2004-04-07 MX MXPA05010398A patent/MXPA05010398A/es active IP Right Grant
- 2004-04-07 JP JP2006500165A patent/JP5111849B2/ja not_active Expired - Fee Related
- 2004-04-07 AU AU2004230294A patent/AU2004230294B2/en not_active Ceased
- 2004-04-07 PL PL377832A patent/PL212544B1/pl unknown
- 2004-04-07 KR KR1020057019123A patent/KR100722079B1/ko not_active IP Right Cessation
- 2004-04-07 CN CNB200480009239XA patent/CN100337996C/zh not_active Expired - Fee Related
- 2004-04-07 GE GEAP20049046A patent/GEP20074257B/en unknown
- 2004-04-07 BR BRPI0409095A patent/BRPI0409095B1/pt not_active IP Right Cessation
- 2004-04-07 CA CA2521877A patent/CA2521877C/fr not_active Expired - Fee Related
- 2004-04-07 EA EA200501557A patent/EA008929B1/ru not_active IP Right Cessation
- 2004-04-07 WO PCT/FR2004/000857 patent/WO2004092095A1/fr active Application Filing
- 2004-04-07 AR ARP040101173A patent/AR043993A1/es not_active Application Discontinuation
- 2004-04-08 MY MYPI20041284A patent/MY138698A/en unknown
- 2004-07-04 UA UAA200510564A patent/UA80040C2/uk unknown
-
2005
- 2005-09-19 MA MA28504A patent/MA27633A1/fr unknown
- 2005-10-09 EG EGNA2005000629 patent/EG24152A/xx active
- 2005-11-09 NO NO20055257A patent/NO334199B1/no not_active IP Right Cessation
-
2006
- 2006-06-19 HK HK06106955A patent/HK1086816A1/xx not_active IP Right Cessation
-
2007
- 2007-01-05 US US11/649,980 patent/US7323575B2/en not_active Expired - Fee Related
Also Published As
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
PSEA | Patent sealed | ||
RENW | Renewal (renewal fees accepted) | ||
RENW | Renewal (renewal fees accepted) | ||
RENW | Renewal (renewal fees accepted) |
Free format text: PATENT RENEWED FOR 3 YEARS UNTIL 07 APR 2017 BY AJ PARK Effective date: 20140203 |
|
RENW | Renewal (renewal fees accepted) |
Free format text: PATENT RENEWED FOR 1 YEAR UNTIL 07 APR 2018 BY AJ PARK Effective date: 20170404 |
|
LAPS | Patent lapsed |